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Hereditary cystic renal diseases (ciliopathies)
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Autosomal dominant tubulointerstitial kidney disease (ADTKD)
UMOD-related autosomal dominant tubulointerstitial kidney disease (ADTKD)
MUC1-related autosomal dominant tubulointerstitial kidney disease (ADTKD)
REN-related autosomal dominant tubulointerstitial kidney disease (ADTKD, FJHN type 1)
HNF1B-related autosomal dominant tubulointerstitial kidney disease (ADTKD)
Autosomal dominant polycystic kidney disease (ADPKD)
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (ADPKD-TSC)
Tuberous sclerosis complex (TSC)
Von Hippel-Lindau disease (vHL)
Autosomal recessive polycystic kidney disease (ARPKD)
Nephronophthisis
Infantile nephronophthisis
Juvenile nephronophthisis
Late-onset nephronophthisis
Bardet-Biedl syndrome
Jeune syndrome (ciliopathies)
Joubert syndrome with oculorenal defect
Joubert syndrome with renal defect
OFD (Orofaciodigital) syndrome type 1
Senior-Loken syndrome
Senior-Boichis syndrome
Saldino-Mainzer (conorenal) syndrome
Meckel syndrome (ciliopathies)
Cerebrorenodigital (Meckel-like) syndrome
Cranioectodermal dysplasia (Sensenbrenner syndrome)
Ellis van Creveld syndrome
Alström Syndrome
Renal-hepatic-pancreatic dysplasia
RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysaplasia) syndrome
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome
Karyomegalic interstitial nephritis
Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
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Glomerulopathies
Tubulopathies
Thrombotic microangiopathies
Metabolic nephropathies
Renal or urinary tract malformations
Familial cystic renal diseases
Any rare kidney disease (A-Z)
Patient Information Materials